On-Site CRC for Interventional Trials | GCP & EDC Pro (Riyadh)

PharmaKnowl Consulting; Riyadh; On-site; SAR 90,000 - 150,000; Full time

Job summary

PharmaKnowl Consulting in Riyadh, Saudi Arabia, seeks a Clinical Research Coordinator (CRC) to manage day-to-day trial activities on-site. You will screen participants, enroll them, schedule visits, and coordinate informed consent documentation in line with approved protocols.

Responsibilities include maintaining accurate source documents, data entry per ICH-GCP and SFDA standards, supporting site visits, and preparing regulatory submissions.

Qualifications

• Bachelor’s degree in a medical or health-related field.
• Minimum 1 year of clinical research experience.
• Knowledge of ICH-GCP guidelines.
• Good knowledge of EDC platforms and clinical data entry.
• Fair understanding of GCP and clinical trial procedures.
• Strong organizational and time-management skills.

Responsibilities

• Coordinate day-to-day clinical trial activities on-site in Riyadh.
• Screen participants, enroll them, and schedule visits per protocol.
• Organize and document informed consent processes and source documents.
• Ensure data is collected and managed per GCP and SFDA standards.
• Support investigators during site visits and regulatory submissions.
• Assist with safety reporting and data query resolution.
• Collaborate with cross-functional teams to meet timelines and quality standards.

Skills

Organizational skills

Time management

GCP knowledge

ICH-GCP guidelines

EDC platforms

Education

Bachelor’s degree in medical/health field

Tools

EDC platforms

Job description

PharmaKnowl Consulting in Riyadh, Saudi Arabia, seeks a Clinical Research Coordinator (CRC) to manage day-to-day trial activities on-site. You will screen participants, enroll them, schedule visits, and coordinate informed consent documentation in line with approved protocols.

Responsibilities include maintaining accurate source documents, data entry per ICH-GCP and SFDA standards, supporting site visits, and preparing regulatory submissions.